Adult-onset central nervous system hemophagocytic lymphohistiocytosis: a case report

BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a clinical syndrome with both genetic and acquired causes characterized by elevated cytokine levels, hyperinflammation, and overactivation of lymphocytes and macrophages. It is typically a systemic disease with variable degrees of CNS involveme...

Descripción completa

Detalles Bibliográficos
Autores principales: Pastula, Daniel M., Burish, Mark, Reis, Gerald F., Bollen, Andrew, Cha, Soonmee, Ralph, Jeffrey, Douglas, Vanja C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4606887/
https://www.ncbi.nlm.nih.gov/pubmed/26467435
http://dx.doi.org/10.1186/s12883-015-0470-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4606887/
https://www.ncbi.nlm.nih.gov/pubmed/26467435
http://dx.doi.org/10.1186/s12883-015-0470-6

Ejemplares similares